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肠道微生物群与结核病感染:相互作用及治疗潜力

Gut microbiota and tuberculosis infection: interaction and therapeutic potential.

作者信息

Chai Yinghui, Li Min, Deng Xianping, Ma Congcong, Zhou Nannan, Chen Yanan, Yao Yushan, Li Kang, Gong Wenping, Lei Hong

机构信息

Department of Clinical Laboratory, The Eighth Medical Center of PLA General Hospital, Beijing, China.

Graduate School, Hebei North University, Zhangjiakou, China.

出版信息

Gut Microbes. 2025 Dec;17(1):2531201. doi: 10.1080/19490976.2025.2531201. Epub 2025 Jul 14.

DOI:10.1080/19490976.2025.2531201
PMID:40654283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12269669/
Abstract

Pulmonary tuberculosis (PTB), caused by (MTB), is a serious chronic infectious disease. Although significant progress has been made in the prevention and treatment of MTB, current anti-tuberculosis therapies still face numerous challenges. The human gut microbiota, a complex ecosystem, plays a role in host metabolism, immune regulation, and health maintenance. Recent studies have increasingly highlighted a close relationship between gut microbiota and PTB. The gut microbiota, through the gut-lung axis, mediates the immune processes of PTB, while MTB infection can disrupt the ecological balance of the gut microbiome. This review aims to summarize the changes in gut microbiota among PTB patients and their relationship with clinical manifestations, explore the role of gut microbiota in PTB immunity, and further analyze the potential application of gut microbiota therapy in PTB treatment. The goal is to provide clear direction for future research on gut microbiota and lung diseases and propose new strategies for MTB treatment.

摘要

肺结核(PTB)由结核分枝杆菌(MTB)引起,是一种严重的慢性传染病。尽管在MTB的预防和治疗方面已取得显著进展,但当前的抗结核治疗仍面临诸多挑战。人体肠道微生物群是一个复杂的生态系统,在宿主代谢、免疫调节和健康维持中发挥作用。最近的研究越来越多地强调了肠道微生物群与PTB之间的密切关系。肠道微生物群通过肠-肺轴介导PTB的免疫过程,而MTB感染会破坏肠道微生物组的生态平衡。本综述旨在总结PTB患者肠道微生物群的变化及其与临床表现的关系,探讨肠道微生物群在PTB免疫中的作用,并进一步分析肠道微生物群疗法在PTB治疗中的潜在应用。目的是为未来肠道微生物群与肺部疾病的研究提供明确方向,并提出MTB治疗的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/200bafff653b/KGMI_A_2531201_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/ab0c2fc3e8b7/KGMI_A_2531201_F0001_OC.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/13170c779183/KGMI_A_2531201_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/200bafff653b/KGMI_A_2531201_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/ab0c2fc3e8b7/KGMI_A_2531201_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/abbc827afb95/KGMI_A_2531201_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/6b0bf52552ec/KGMI_A_2531201_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/13170c779183/KGMI_A_2531201_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b7/12269669/200bafff653b/KGMI_A_2531201_F0005_OC.jpg

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Front Immunol. 2025 May 14;16:1561459. doi: 10.3389/fimmu.2025.1561459. eCollection 2025.
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A gut commensal protozoan determines respiratory disease outcomes by shaping pulmonary immunity.一种肠道共生原生动物通过塑造肺部免疫来决定呼吸道疾病的结局。
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Impact of diabetes mellitus on tuberculosis prevention, diagnosis, and treatment from an immunologic perspective.
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Exploration (Beijing). 2024 Mar 5;4(5):20230138. doi: 10.1002/EXP.20230138. eCollection 2024 Oct.
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The interaction of innate immune and adaptive immune system.先天免疫系统与适应性免疫系统的相互作用。
MedComm (2020). 2024 Sep 15;5(10):e714. doi: 10.1002/mco2.714. eCollection 2024 Oct.
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The effect of intestinal flora metabolites on macrophage polarization.肠道菌群代谢产物对巨噬细胞极化的影响。
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